A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477333



Internal ID254918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:127159723..127169635hg38UCSC Ensembl
chr7:126799777..126809689hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg389913
hg199913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003517
Samples
Known GenesGRM8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477333
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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